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FDA 510(k)

MICROPAD

K-Number: K823301 · 1982-12-03

ApplicantFia Man Co.
Decision Date1982-12-03
Product CodeIRT
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MICROPAD is the device name listed in this FDA 510(k) record. The listed applicant is Fia Man Co.. It received FDA 510(k) clearance on 1982-12-03 under 510(k) number K823301. The device is classified under product code IRT. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROPAD?

MICROPAD is a medical device that received FDA 510(k) clearance on 1982-12-03. The listed applicant is Fia Man Co.. The 510(k) number is K823301.

When did MICROPAD receive FDA 510(k) clearance?

MICROPAD received FDA 510(k) clearance on 1982-12-03, under 510(k) number K823301.

Who is the listed applicant for MICROPAD?

The FDA 510(k) record lists Fia Man Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROPAD?

The FDA product code for MICROPAD is IRT.

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Related Devices (Code: IRT)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K250047bite away twomibeTec GmbHK220514bite away neomibeTec GmbHK160943Bite AwayRiemser PharmaK111273FIR HEAT THERAPHY SYSYEMSShenzhen Anpan Technology Co., Ltd.K072534BIO-MAT 2000Richway Intl., Inc.K963887PT-PAC PORTABLE HEATING PADAnthony A. Chiurco

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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